ClearanceBrief
510(k) K001926 ยท DYB Introducer, Catheter

VASCULAR GRAFT TUNNELER-STANDARD CURVE, MID CURVE, FULL CURVE, SHORT STANDARD CURVE, VASCULAR GRAFT TUNNELER ACCESSORIES

ApplicantThoratec Laboratories Corp., Pleasanton CA, US
DecisionSubstantially Equivalent, Sep 22, 2000
ReceivedJun 26, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001926

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.